戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2390468作成日:2026年10月26日

Ammonium Chloride → 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole

https://huagongshe.com/reaction/2390468

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物N1-Methyl-4-(trifluoromethyl)benzene-1,2-diamineHCID 715666—
反応物3-FluoroisonicotinaldehydeHCID 2763003—
反応物Sodium BisulfiteHCID 23665763—
溶媒DimethylformamideHCID 6228—
生成物2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazoleHCID 6661152262%

反応条件

温度80 °C

反応手順

A mixture of 1.90 g of N1-methyl-4-trifluoromethylbenzene-1,2-diamine, 1.49 g of 3-fluoropyridine-4-carbaldehyde, 3.12 g of sodium bisulfite and 20 ml of DMF was stirred for 1.5 hours while heating at 80° C., then, was stirred for 2 hours while heating at 120° C. After cooling down to room temperature, a saturated ammonium chloride aqueous solution was poured, and the mixture was extracted three times with ethyl acetate. The combined organic layers were dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.83 g of 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273764B2
出典データセットuspto-grants-2012_09
ORD IDord-322696cc977e4e8d843e9d0710be5298
出典メモuspto-grants-2012_09